Stackable spinal support system

ABSTRACT

A method for distracting two tissue surfaces away from one another within a spine. In one embodiment, the method involves the steps of: (a) providing a plurality of biocompatible and generally rectangular spinal inserts having a generally planar top surface having a leading edge and a trailing edge, a generally planar bottom surface disposed generally parallel to the top surface and including a leading edge and a trailing edge, and a beveled surface extending from at least one of the leading edge of the planar top surface and the leading edge of the planar bottom surface; and (b) successively introducing into a spine the plurality of spinal inserts such that the generally planar top and bottom surfaces are generally parallel to the two tissue surfaces, wherein the beveled surface are configured to allow a currently inserted spinal insert to be positioned at least one of above and below a previously introduced spinal insert to distract the two tissue surfaces.

CROSS REFERENCES TO RELATED APPLICATIONS

The present application claims priority from commonly owned and co-pending U.S. patent application Ser. No. 11/053,016, filed Feb. 8, 2005, which claims priority from U.S. patent application Ser. No. 09/904,179 filed Jul. 11, 2001, now issued as U.S. Pat. No. 6,852,126, which claims benefit under 35 U.S.C. §119(e) from U.S. Provisional Application Ser. No. 60/218,975, filed Jul. 17, 2000, the entire contents of which are hereby expressly incorporated by reference into this disclosure as if set forth fully herein.

BACKGROUND OF THE INVENTION

The present invention provides a stackable interlocking intervertebral support system, and methods for supporting adjacent vertebrae using a stackable interlocking intervertebral support system.

In preferred aspects, the present invention comprises two, three (or more) separate portions which are stacked together to form an interlocked intervertebral support assembly. Advantageously, two of these three (or more) portions may be identical in size and shape, as will be explained. In the optional aspect of the invention in which only two separate portions are used, these two portions may be identical to one another in size and shape.

In one preferred aspect, the present invention preferably comprises a center portion, a top portion and a bottom portion. The top portion is positioned on top of the center portion and the bottom portion is positioned under the center portion. The top and bottom portions may be identically shaped and dimensioned, but are positioned upside down with respect to one another, on opposite sides of the center portion, as will be explained. In another aspect of the invention, however, only two portions are used, with the top portion being positioned directly on top of the bottom portion (with no center portion(s) required). In further aspects of the present invention, more than three separate portions may be used. In such aspects, a plurality of identically shaped center portions are stacked one on top of the other. In other alternate aspects, various portions (including top, center and bottom portions) may be stacked side by side one another).

In accordance with the present invention, the center portion has a recess in each of its top and bottom surfaces. Each of the top and bottom portions of the present system also have recesses therein which engage and interlock with the recesses in the center portion. More specifically, the top portion preferably has a recess in its bottom surface and the bottom portion has a recess in its top surface which engage the respective recesses in the top and bottom of the center portion.

The present invention is assembled simply by stacking the three portions (top, center & bottom) one on top of one another in a patient's intervertebral space. When stacked together, the present assembly will form an “X” or “cross” type of shape, providing support over a large surface area of the adjacent vertebrae. In further optional aspects of the invention, more than three portions are stacked together one on top of one another in a patient's intervertebral space. Specifically, a plurality of center portions are stacked on a bottom portion and a top portion is stacked thereover.

A further advantage of the present system is that, when assembled, it provides support in two perpendicular directions, thereby supporting a large area of the adjacent vertebrae, yet using only a minimal amount of material in actually achieving this advantage. This advantage is due, at least in part, to the assembled “cross” shape of the assembly. Moreover, the present invention can be dimensioned to be of a size such that the “arms” of the “cross” extend outwardly towards the edges of the vertebrae, providing support over the cortical bone at the vertebral edges.

Another advantage of the present invention is that, as the adjacent vertebrae tend to push together, this will hold the present support assembly together, even in the absence of any mechanical fastening or securing mechanisms between the top, center & bottom portions of the system. Specifically, both (one or more) center portion(s) and the two top/bottom portions are uniquely shaped and dimensioned such that when positioned one on top of another, they will remain firmly together, resisting any lateral tendency to slip apart.

Yet another advantage of the present invention is that it may be easily inserted into a patients's intervertebral space in a bi-portal minimally invasive surgical approach. Specifically, the bottom portion may be inserted through a first cannula into the patient's intervertebral space, with the center portion(s) thereafter being inserted through a second cannula into the patient's intervertebral space. The top portion may then be inserted through the first cannula into the patient's intervertebral space. In this aspect of the invention, the first and second cannula are generally perpendicular to one another, being positioned in opposite posterolateral approaches. Alternatively, all of the portions of the assembly may be inserted through the same operating cannula into the patient's intervertebral space, with successive portions then rotated perpendicular to one another after they have been positioned in the patient's intervertebral space.

In preferred aspects, each of the center, top and bottom portions of the assembly have a tapered end, which is dimensioned to engage a ramping structure disposed within one of the recesses on an adjacent portion such that the separate portions of the assembly may be “slip-fit” together, with pressure between the adjacent vertebrae holding each of the pieces of the assembly together. In addition, an optional tapered front end of the center portion may be used to pry apart the adjacent vertebrae, prior to positioning the top portion thereover.

In optional aspects of the invention, a plurality of the present support assemblies can be positioned in a patient's intervertebral space, either on top of, beside or both on top of and beside, one another.

BRIEF DESCRIPTION OF THE DRAWINGS

Many advantages of the present invention will be apparent to those skilled in the art with a reading of this specification in conjunction with the attached drawings, wherein like reference numerals are applied to like elements and wherein;

FIG. 1 is an exploded front/side perspective view of an exemplary arrangement of the present stackable interlocking intervertebral support system;

FIG. 2 is a top front/side perspective view of the exemplary arrangement of the present system seen in FIG. 1;

FIG. 3 is a bottom front/side perspective view of the exemplary arrangement of the present system seen in FIG. 1;

FIG. 4 is a top plan view of the exemplary arrangement of the present system seen in FIG. 1;

FIG. 5 is a front/side elevation view of the exemplary arrangement of the present system seen in FIG. 1, (shown in two adjacent vertebrae in an exploded view);

FIG. 6 is a rear elevation view of the exemplary arrangement of the present system seen in FIG. 1;

FIGS. 7A, 7B and 7C are front perspective views of the center portion of the present system;

FIG. 8 is a rear perspective view of the center portion of the present system;

FIG. 9A is a top plan view of the center portion of the present system;

FIG. 9B corresponds to FIG. 9A, but has center ramp/recesses angled to a lateral axis across the center portion;

FIG. 10 is a side elevation view of the center portion of the present system;

FIG. 11 is a front elevation view of the center potion of the present system;

FIG. 12 is a top front perspective view of the bottom portion of the present system, (or is a bottom perspective view of the top portion of the present system);

FIG. 13 is a top rear perspective view of the bottom portion of the present system, (or is a bottom perspective view of the top portion of the present system);

FIG. 14 is a bottom rear perspective view of the bottom portion of the present system;

FIG. 15 is a top plan view of a bottom portion of the present system;

FIG. 16 is a side elevation view of the bottom portion of the present invention;

FIG. 17 is a front elevation view of the bottom portion of the present invention;

FIG. 18 is a top perspective view of a patient's intervertebral space showing the positioning of the present system (with one vertebra shown in phantom);

FIG. 19 is a top plan view of a patient's intervertebral space showing posterolateral approaches used in positioning the separate portions of the present system;

FIG. 20 is an exploded perspective view of a patient's intervertebral space showing an assembly comprising four portions, (including two center portions, a top portion and a bottom portion) positioned one on top of the other, and

FIG. 21 is an exploded perspective view of a two-portion intervertebral support assembly.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

Illustrative embodiments of the invention are described below. In the interest of clarity, not all features of an actual implementation are described in this specification. It will of course be appreciated that in the development of any such actual embodiment, numerous implementation-specific decisions must be made to achieve the developers' specific goals, such as compliance with system-related and business-related constraints, which will vary from one implementation to another. Moreover, it will be appreciated that such a development effort might be complex and time-consuming, but would nevertheless be a routine undertaking for those of ordinary skill in the art having the benefit of this disclosure. The stackable interlocking intervertebral support system disclosed herein boasts a variety of inventive features and components that warrant patent protection, both individually and in combination.

Referring first to FIG. 1, an exploded front side perspective view of the present stackable interlocking intervertebral support system 5 is provided. In one preferred arrangement, system 5 comprises a center portion 10, a bottom portion 20A and a top portion 20B. (As will be explained, other arrangements are possible). As can be seen throughout the attached Figs., portions 20A and 20B may preferably be identical in shape and size. Accordingly, the present system 5 may actually comprise one center portion 10 and two top/bottom portions 20.

FIGS. 2 and 3 show respective top and bottom perspective views of the present systems in an assembled format. As will be explained, an advantage of the present system is that it provides support between adjacent vertebrae without requiring any mechanical fastening systems between the top, center and bottom portions of the assembly. Rather, center portion 10, bottom portion 20A and top portion 20B are all assembled together with their novel shapes assisting in keeping them together.

Referring to the attached Figs., (and to FIGS. 7A to 10 in particular), center potion 10 is provided with bottom recess 11A and top recess 11B, passing thereacross, as shown. Also referring to the attached Figs., (and to FIGS. 13 to 16 in particular), bottom portion 20A is also proved with a top recess 21A. (Conversely, being identically shaped to bottom portion 20A, top portion 20B is also provided with a bottom recess 21B).

An important aspect of the present invention is that, when bottom portion 20A is positioned below center portion 10, recess 21A will engage and interlock with recess 11A. Conversely, when top portion 20B is positioned on top of center portion 10, recess 21B will engage and interlock with recess 11B. Accordingly, when center portion 10, bottom portion 20A and top portion 20B are stacked together, recesses 11 will engage recesses 21, such that assembly 5 forms an “X” or “cross” shape. As can be seen, recesses 11 and 21 are preferably positioned mid-way (ie: centrally) along the respective lengths of portions 10 and 20. As illustrated, assembly 5 will have an “X” shape with each of the four branches of the “X” being relatively equal in length. Within the scope of the present invention, however, recesses 11 and 21 may instead be positioned closer to one end of their respective potions than another, such that the “X” shape of the present assembly will instead have two of its branches longer than another two of its branches (and may even approach a “V” shape assembly). Moreover, the angles at which recesses 11 and 21 cut laterally across portions 10 and 20 can be angled as denoted by angle “α” in FIG. 9B (for center portion 10). As such, when stacked together, the angles between each of the 4 “arms” of the “X” of the present assembly need not be perpendicular to one another. (For example, 2 pairs of arms may be 60° apart, with the other 2 pairs of arms being 120° apart).

As can be seen throughout the attached Figs., center portion 10 has a bottom surface 12 and a top surface 14. Bottom portion 20A has a bottom surface 22A, and top portion 20B has a top surface 22B. When the three portions of the present assembly are assembled, surface 14 is coplanar with surface 22B and surface 12 is coplanar with surface 22A. As shown in FIG. 5, surfaces 12 and 22A together support (ie: butts against) vertebra 50 and surfaces 14 and 22B together support (ie: buttress against) an opposite adjacent vertebra 52. (For illustration purposes only, opposite adjacent vertebrae 50 and 52 are shown in an exploded view). It is to be understood that after distraction vertebrae 50 and 52 will tend to move toward one another, applying pressure to the top and bottom of assembly 5, keeping assembly 5 together. As can be seen, surfaces 12, 14, 22A, and 22B may all have a plurality of small groves 23 (or other surface irregularities) which increases sliding fiction across these surfaces.

A further advantage of the novel shape of center portion 10 is that it has a tapered front end 13. In a preferred method of assembling the present support assembly 5, as illustrated in FIGS. 18 and 19, center portion 10 is advanced minimally invasively into patient P in a posterolateral approach through cannula 60 and positioned between opposite adjacent vertebrae 50 and 52 (shown here as being on top of vertebra 50). Tapered end 13 will tend to pry apart adjacent vertebrae 50 and 52, providing the surgeon with a “self-distracting” vertebral support system. Bottom portions 20A and top portions 20B are advanced through minimally invasive cannula 62 in an opposite posterolateral approach. Typically, bottom portion 20A is positioned first, followed by center portion 10 and top portion 20B stacked sequentially thereover.

Each of center portion 10 and top portion 20B also have tapered front ends 13 and 25 which (as center portion 10 and top portion 20B are sequentially slipped over bottom portion 10 and center portion 10), will engage ramp structures 17 disposed within recesses 21A and 11A in respective bottom portion 20A and center portion 10, such that center portion 10 and top portion 20B are “snap-fitted” over bottom portion 20A. More specifically, during insertion, vertebrae 50 and 52 will tend to rest against surfaces 12 and 14 of center portion 10. As center portion(s) 10 and top portion 20B are “snap-fitted” over bottom portion 20A and center portion 10, their respective tapered ends 13 and 25 will assist in urging vertebrae 50 and 52 apart. When assembled, ramp structures 27 disposed within recesses 21A and 21B will interlock with engage ramp structures 17 in center portion 10, such that assembly 5 will be held together, by intervertebral pressure (on surfaces 14 and 22B, and surfaces 12 and 22A) urging vertebrae 50 and 52 together.

Portions 10 and 20 of the present invention may preferably each have a narrow elongated shape, as shown. Accordingly, they may be dimensioned to be small enough to pass through an operating cannula, for example, an operating cannula having an interior diameter equal to, or less than, 8 mm or 6 mm.

In preferred aspects of the invention, portions 10 and 20 are preferably made of bone allograft material, offering the advantages of promoting healing and eventual absorption of system 5. Alternatively, portions 10 and 20 may be made of metal, or any other suitable bio-implantable material. Each of center portion 10, and top/bottom portion 20 may optionally have side grooves 15 and 25 in which opposite prongs 42 of a two prong inserter 40 (such as a “pinching” inserter as shown in FIGS. 7A and 13) which may be used when inserting each of center portion 10 and top/bottom portions 20 through respective surgical cannulae 60 and 62.

If desired, the vertical height of the present system can be increased by stacking more than one center portion 10 (as shown in FIG. 20 in which an assembly 5A is shown having two center portions 10). It is to be understood that more than two center portions 10 may be used in assembling the present intervertebral support system, as desired. In yet another optional aspect of the invention, assemblies 5 may be made small enough such that more than one can be positioned side by side in a patient's intervertebral space. As is seen in FIG. 21, a two portion intervertebral support assembly 5B is also contemplated. In this aspect of the invention, top portion 20B is positioned directly on top of bottom portion 20A, with recesses 21A and 21B interlocking together. Many other system arrangements are possible. For example, two, or more than two portions 10 can be staked on top of one another (similar to the stacking of portions 20 in FIG. 21). 

What is claimed is:
 1. A method for distracting two tissue surfaces away from one another within a spine, comprising: introducing into a spine a plurality of biocompatible spinal inserts configured to form a vertically stacked and interlocked support, said plurality of biocompatible spinal inserts including a top insert, a center insert and a bottom insert, said center insert including a tapered leading end, a ramp, an upper recess, a lower recess, an upper facing surface and a lower facing surface generally parallel to the upper facing surface, said top insert including a ramp configured to engage the tapered leading end of the center insert to assist in distraction of the two tissue surfaces, a recess configured to engage and interlock with the upper recess of the center insert, an upper facing surface configured to be positioned against a first tissue surface and a lower facing surface configured to contact the upper facing surface of the center insert, said bottom insert including a recess configured to receive a portion of the center insert, an upper facing surface configured to contact the lower facing surface of the center insert and a lower facing surface configured to be positioned against a second tissue surface.
 2. The method of claim 1, further comprising a sub-step of introducing said plurality of biocompatible spinal inserts via an introduction instrument configured to pass each of said plurality of spinal inserts into the spine.
 3. The method of claim 2, wherein each of the plurality of biocompatible spinal inserts include a feature configured to facilitate coupling to said introduction instrument.
 4. The method of claim 1, wherein a plurality of center inserts are introduced into the spine.
 5. The method of claim 4, wherein the plurality of center inserts are introduced into the spine after the bottom insert.
 6. The method of claim 1, wherein the plurality of biocompatible spinal inserts are dimensioned to provide support over cortical bone edges of a vertebral body.
 7. The method of claim 1, wherein the plurality of biocompatible spinal inserts are introduced into the spine from a posterolateral approach.
 8. The method of claim 1, wherein the plurality of biocompatible spinal inserts are introduced into the spine via a single approach.
 9. The method of claim 1, wherein the plurality of biocompatible spinal inserts are introduced into the spine via a minimally invasive approach.
 10. The method of claim 1, wherein the bottom insert is introduced into the spine first, followed sequentially by the center insert and the top insert.
 11. The method of claim 1, wherein a first plurality of biocompatible spinal inserts configured to form a first vertically stacked and interlocked support is introduced into an intervertebral space, and a second plurality of inserts configured to form a second vertically stacked and interlocked support is introduced into the intervertebral space and positioned side by side with the first plurality of biocompatible inserts.
 12. A method for increasing a distance between two tissue surfaces within a spine, comprising: (a) introducing into a human spine a first biocompatible spinal insert having a ramp, a lower surface including a recess, an upper surface generally parallel to said lower surface; and (b) introducing into the human spine a second biocompatible spinal insert having a tapered leading end, an upper surface having a recess configured to engage and interlock with the recess of the first spinal insert, a lower surface generally parallel to the upper surface, wherein the tapered leading end of the second spinal insert contacts the ramp of the first spinal insert during introduction such that said second spinal insert is positioned in a vertically stacked configuration with said first spinal insert so as to increase said distance between said two tissue surfaces within said spine.
 13. The method of claim 12, wherein steps (a) and (b) each include the further sub-step of introducing said first and second biocompatible spinal inserts via an introduction instrument configured to pass each of said first and second biocompatible spinal inserts into the spine.
 14. The method of claim 13, wherein each of said first and second biocompatible spinal inserts include a feature configured to facilitate coupling to said introduction instrument.
 15. The method of claim 12, wherein steps (a) and (b) each involve introducing said first and second biocompatible spinal inserts into an intervertebral space of the spine.
 16. The method of claim 15, wherein each of said first and second biocompatible spinal inserts are sequentially stacked in the intervertebral space of the spine.
 17. The method of claim 12, wherein said first and second biocompatible spinal inserts are sequentially stacked in an intervertebral space of the spine.
 18. The method of claim 12, wherein the first and second biocompatible spinal inserts are dimensioned to provide support over cortical bone edges of a vertebral body.
 19. The method of claim 12, wherein the first and second biocompatible spinal inserts are introduced into the patient's spine from a posterolateral approach.
 20. The method of claim 12, wherein the first and second biocompatible spinal inserts are introduced into the patient's spine via a single approach.
 21. The method of claim 12, wherein the first and second biocompatible spinal inserts are introduced into the patient's spine via a minimally invasive approach. 